US8372519B2 - Composition and method for treating wood - Google Patents
Composition and method for treating wood Download PDFInfo
- Publication number
- US8372519B2 US8372519B2 US12/434,724 US43472409A US8372519B2 US 8372519 B2 US8372519 B2 US 8372519B2 US 43472409 A US43472409 A US 43472409A US 8372519 B2 US8372519 B2 US 8372519B2
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- United States
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- composition
- wood
- thiol
- ene
- wood element
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- 239000000203 mixture Substances 0.000 title claims abstract description 193
- 239000002023 wood Substances 0.000 title claims abstract description 164
- 238000000034 method Methods 0.000 title abstract description 46
- 125000003396 thiol group Chemical class [H]S* 0.000 claims abstract description 30
- 150000003573 thiols Chemical class 0.000 claims description 68
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
- 239000003999 initiator Substances 0.000 claims description 11
- -1 allyl ethers Chemical class 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 9
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical class CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 8
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 8
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 8
- 150000001336 alkenes Chemical class 0.000 claims description 8
- 150000001993 dienes Chemical class 0.000 claims description 8
- 239000003112 inhibitor Substances 0.000 claims description 8
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims description 8
- 239000000049 pigment Substances 0.000 claims description 8
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical class OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 7
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 claims description 7
- 239000011121 hardwood Substances 0.000 claims description 7
- 229920001567 vinyl ester resin Polymers 0.000 claims description 7
- 239000000975 dye Substances 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 4
- 239000011122 softwood Substances 0.000 claims description 4
- 238000005470 impregnation Methods 0.000 description 36
- 238000012360 testing method Methods 0.000 description 29
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 24
- OXBLVCZKDOZZOJ-UHFFFAOYSA-N 2,3-Dihydrothiophene Chemical compound C1CC=CS1 OXBLVCZKDOZZOJ-UHFFFAOYSA-N 0.000 description 21
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 19
- 238000005452 bending Methods 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 230000008569 process Effects 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 14
- 241000219495 Betulaceae Species 0.000 description 12
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 12
- 235000018185 Betula X alpestris Nutrition 0.000 description 11
- 235000018212 Betula X uliginosa Nutrition 0.000 description 11
- 241001070947 Fagus Species 0.000 description 11
- 235000010099 Fagus sylvatica Nutrition 0.000 description 11
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 11
- 229940113165 trimethylolpropane Drugs 0.000 description 11
- 239000007788 liquid Substances 0.000 description 9
- VLCCKNLIFIJYOQ-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] 2,2,3,3-tetrakis(sulfanyl)propanoate Chemical compound OCC(CO)(CO)COC(=O)C(S)(S)C(S)S VLCCKNLIFIJYOQ-UHFFFAOYSA-N 0.000 description 8
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 125000000524 functional group Chemical group 0.000 description 6
- 238000011835 investigation Methods 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- 241000894007 species Species 0.000 description 6
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 5
- 241000519995 Stachys sylvatica Species 0.000 description 5
- 230000006835 compression Effects 0.000 description 5
- 238000007906 compression Methods 0.000 description 5
- 230000035515 penetration Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 230000001276 controlling effect Effects 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 230000036632 reaction speed Effects 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- 241000183024 Populus tremula Species 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000012505 colouration Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002383 tung oil Substances 0.000 description 2
- 0 *S.*S*S.*SCC(C)C(C)C*S.*[S].*[S].*[S].*[S].*[S].*[S].C=CC.CC(S)C*S.CCC*S.CCC*S.CCC*S.CCC*S.CCC*S.[2HH].[H]*S.[H]C(C)C*S Chemical compound *S.*S*S.*SCC(C)C(C)C*S.*[S].*[S].*[S].*[S].*[S].*[S].C=CC.CC(S)C*S.CCC*S.CCC*S.CCC*S.CCC*S.CCC*S.[2HH].[H]*S.[H]C(C)C*S 0.000 description 1
- OGBWMWKMTUSNKE-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C OGBWMWKMTUSNKE-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 description 1
- 238000006596 Alder-ene reaction Methods 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000218657 Picea Species 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 150000001356 alkyl thiols Chemical class 0.000 description 1
- JQRRFDWXQOQICD-UHFFFAOYSA-N biphenylen-1-ylboronic acid Chemical compound C12=CC=CC=C2C2=C1C=CC=C2B(O)O JQRRFDWXQOQICD-UHFFFAOYSA-N 0.000 description 1
- 238000009435 building construction Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000001048 orange dye Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/02—Processes; Apparatus
- B27K3/15—Impregnating involving polymerisation including use of polymer-containing impregnating agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K5/00—Treating of wood not provided for in groups B27K1/00, B27K3/00
- B27K5/02—Staining or dyeing wood; Bleaching wood
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/04—Polythioethers from mercapto compounds or metallic derivatives thereof
- C08G75/045—Polythioethers from mercapto compounds or metallic derivatives thereof from mercapto compounds and unsaturated compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/12—Polythioether-ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/02—Polythioethers; Polythioether-ethers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31975—Of cellulosic next to another carbohydrate
- Y10T428/31978—Cellulosic next to another cellulosic
- Y10T428/31986—Regenerated or modified
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31989—Of wood
Definitions
- the present invention relates to a composition in the form of a mixture comprising at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, a composition in batch form comprising at least two components a) and b), wherein the component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, and finally, an impregnated wood element obtainable by impregnation of a wood element with the composition and a method of impregnation.
- Thiol-ene free radical chemistry is known from early works that are dated back to late 1930s. A review “Thiol-Enes: Chemistry of the Past with Promise for the Future” is written by Charles E. Hoyle, Tai Yeon Lee, Todd Roper in J. Polym. Sci. Part A: Polym. Chem.: Vol. 42 (2004). Thiolenes have been used in the following fields: clear protective coatings, pigmented coatings, photoinitiated liquid crystalline structural materials and adhesives.
- Impregnation/modification of wood is described in many applications and patents.
- the main objective in these applications has been to prevent the wood from degradation and fungi by improving the water resistance.
- Focus for the last years has been to replace old impregnation methods with new, environmental friendly techniques.
- Several promising techniques are based on treating wood with furfuryl (WPT/Kebony), acetyl (Accoya/Accsys/Titanwood), phenol (Fibron, C-K composites, Permali etc) or urea/melanin/formaldehyde resin (BASF/Belmadur).
- Water/aqueous based impregnation techniques depend largely on controlled swelling of the wood cells during an energy intensive process including high temperature and pressure over time. Several of the techniques show good performance with improved water resistance, but none have so far proved to be cost efficient. Common drawbacks are also limited penetration of the impregnation liquid, discolouring and to some extent swelling of the impregnated wood products.
- Impregnation with organic oils like Tung and Linseed oil has historically been the preferred impregnation technique for wood.
- the oils depend on a slow air oxidation mechanism to cure properly. Penetration is limited, often resulting in an incomplete water resistance.
- Wood is a preferred material for furniture productions.
- massive wood constructions have limited mechanical strength compared to materials like metal and various composite materials. Furniture designers are therefore forced to use other materials when thin constructions are required.
- the objective of the present invention is to provide an impregnated wood element with improved properties and performance in different applications, such as water resistance, hardness, dimension stability, mechanical strength, stiffness, high E module and colouration. This is achieved with a composition which is used for impregnating wood elements.
- the present invention relates to a composition in the form of a mixture comprising at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, wherein the molar ratio between the thiol groups and the ene groups is 1:0.1 to 1:100.
- the present invention relates to a composition in batch form (multi-component form) comprising at least two components a) and b), wherein the component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, wherein the molar ratio between the thiol groups and the ene groups is 1:0.1 to 1:100, and the components a) and b) are separated from each other.
- an impregnated wood element obtainable by impregnating a wood element with a composition in the form of a mixture according to the present invention or a mixture of the components of the composition in batch form (multi-component form) according to the present invention, and thereafter curing the composition or the mixture is also included in the invention.
- the present invention relates to a method of impregnating wood, wherein the wood element is impregnated with the composition in the form of a mixture according to the present invention or a mixture of the components of the composition in batch form (multi-component form) according to the present invention.
- compositions in the form of a mixture or a mixture of the components of the composition in batch form for impregnating wood elements is also concerned.
- thiol is meant a compound that contains the functional group composed of a sulphur atom and a hydrogen atom, i.e. a —SH group. This functional group is referred to as either a thiol group or a sulphydryl group. Thiols are also referred to as mercaptans.
- ene is meant a compound that contains at least one functional group composed of an unsaturation that is a double bond or a triple bond between two carbon atoms. This functional group is referred to as an ene group.
- “Mono functional” means one molecule having one functional group. When relating to thiols, it would mean a thiol molecule having one thiol group. The same is valid for enes, i.e. the molecule has one unsaturation.
- Multi functional means one molecule having two or more functional groups. When relating to thiols, it would mean a thiol molecule having two or more thiol groups. The same is valid for enes, i.e. the molecule has two or more unsaturations.
- Thiol-enes is the expression for a solution comprising compounds having thiol groups and compounds having ene groups. This expression may be used sometimes for the composition comprising the two components a) and b). But it can only be used when the components a) and b) are in mixture.
- composition in batch form (multi-component form) is used in the application.
- batch form is meant that for example at least two components are comprised in the composition and they are held separate from each other. They can be separated by being kept in two separate vessels or in a vessel having a partition wall, which can be withdrawn or broken later on, when the composition is to be used. The separation may be used, for two components that would react when not desired, for example when two components react before it is applied in the impregnation process. This depends on which components which are chosen and what storage time is desired.
- composition in the form of a mixture is used when the at least two components are in mixture in the composition.
- a wood element may be any piece or part of a wood, compressed or uncompressed, of hardwood, softwood or any type of wood species.
- the present invention relates to a composition in the form of a mixture comprising at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, wherein the molar ratio between the thiol groups and the ene groups is from 1:0.1 to 1:100.
- the different molar ratios between thiol and ene enables the operator to control the curing process and tailor make the impregnated wood element properties.
- Another effective conversion of the reactive thiol groups and ene groups is achieved for molar ratios of thiol and ene ranging from 1:0.9 to 1:10.
- the thiol is to a large extent acting as an initiator and chain transfer agent, at higher ratios the thiol is to a larger extent acting as a co-monomer.
- the composition is used for impregnating wood. Very good penetration is achieved by using an ordinary vacuum-pressure impregnation autoclave. Curing is achieved at 60-150 degrees C. adding any ordinary heat source like a heat oven, a wood drying kiln/chamber, a HF/warm press etc. The resulting wood element will have significantly increased mechanical properties.
- Nordic hard wood species like alder, beech and birch will after impregnation all have hardness in the range 8-15 Brinell depending on the initial wood texture (annual ring orientation, knots, initial hardness etc).
- Tests of bending strength show increased values up to 70% for the same species.
- the bending strength for birch increased from 115 MPa to 160 MPa and for compressed birch the bending strength increased from 141 MPa to 239 MPa (see table 8, Example 9).
- the invention relates to a composition in batch form comprising at least two components a) and b), wherein the component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, wherein the molar ratio between the thiol groups and the ene groups is 1:0.1 to 1:100, and the components a) and b) are separated from each other.
- the components sometimes need to be separated, since the thiol groups and the ene groups may react with each other before it is desired. Some of the mixtures of the components a) and b) react very quickly, while other mixtures of two components a) and b) may not react that fast.
- Such a mixture or composition has a longer pot life. It should be understood that a mixture of the two components a) and b) in the composition of the batch form is the equivalence to the composition in the form of a mixture comprising the two components a) and b).
- a regular and controllable polymer network can be obtained by the narrower range.
- the degree of curing may also be improved.
- composition relates to both composition in the form of a mixture and composition in batch form if not other specified.
- compositions with thiol groups and ene groups are earlier known, and are often referred to as “thiol-enes” as mentioned above.
- the use area for thiol-enes has been clear protective coatings, pigmented coatings, photo-initiated liquid crystalline structural materials and adhesives.
- the composition comprises at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol and component b) comprises at least one mono and/or multifunctional ene, wherein the molar ratio between the thiol groups and the ene groups is 1:0.1 to 1:100 is possible to use for impregnation of wood elements and give wood elements with very good properties. Besides, the area of application of wood may be increased. The molar ratio between the thiol groups and the ene groups may also be 1:0.9 to 1.10.
- composition in the form of a mixture comprising a component comprising at least one mono and/or multifunctional thiol group and a component comprising at least one mono and/or multifunctional ene group according to the present invention can be cured through a free radical mechanism (see scheme 1 below) at room temperature.
- the overall conversion rate of the thiol-ene reaction is directly related to the electron density on the ene, with an electron rich ene consumed much more quickly than electron poor enes.
- the basic exception to this rule is that highly conjugated double bonds copolymerise very slowly with thiols.
- the ordering of reactivity for different enes with thiols is shown in Scheme 2 below.
- Thiols based on mercaptopropionate esters co-polymerise with a given ene more quickly than mercaptoacetate esters, which in turn react more quickly than simple alkyl thiols.
- a composition in the form of a mixture according to the present invention can thus be controlled by selecting different thiol and ene combinations or use inhibitors or free radical initiators. If the reaction is starting too quickly, it may be necessary to use the composition in batch form (multi-component form) and provide a mixture when impregnating wood elements.
- a batch form can provide the different components in different vessels or in a vessel comprising at least two compartments. When the composition shall be mixed, the content from different vessels is mixed or the content of different compartments of a vessel will be mixed. A separation wall between different compartments may be broken or the components can be mixed in a separate vessel. If the components do not react very quickly, there is no problem having the components in one vessel.
- a free radical initiator if the reaction needs to be started when for example it is to slow.
- an inhibitor can be used instead of using different vessels or a partition into different compartments for the components. The reaction between the components will then be inhibited when it is desired.
- the thiols can be selected from the group consisting of mercaptopropionate esters, mercaptoacetate esters and mixtures thereof. These thiols are suitable because they give a pot life and curing process that can be controlled. Also, the properties of the impregnation can be tailor-made.
- the enes may be chosen from the group consisting of norbornene, vinyl ether, propenyl, alkene, vinyl ester, N-vinyl amides, allyl ethers, allyltriazine, allylisocyanurate, acrylate, unsaturated esters, N-substituted meleimide, acrylonitrile, methacrylate, styrene, conjugated dienes and mixtures thereof. These enes are suitable since they give a pot life and curing process that can be controlled. The properties of the impregnation can of course also be tailor-made.
- the invention also relates to a composition in batch form comprising at least two components a) and b), wherein the component a) comprises at least one mono and/or multifunctional thiol selected from the group consisting of mercaptopropionate esters, mercaptoacetate esters and mixtures thereof, and component b) comprises at least one mono and/or multifunctional ene chosen from the group consisting of norbornene, vinyl ether, propenyl, alkene, vinyl ester, N-vinyl amides, allyl ethers, allyltriazine, allylisocyanurate, acrylate, unsaturated esters, N-substituted meleimide, acrylonitrile, methacrylate, styrene, conjugated dienes and mixtures thereof, the molar ratio between the thiol groups and the ene groups is 1:0.1 to 1:100; and the components a) and b) are separated from each other.
- At least one of the components a) and b) may comprise dyes, micronised pigments and/or pigments.
- the dyes will be preferred due to its small size and high penetration giving a controllable colouring process.
- At least one of the components a) and b) may comprise additives selected from initiators, inhibitors, and other additives.
- Initiators and inhibitors can control the reaction.
- the initiators can be activated by for example heat (IR, convection, microwave), photo (UV/Visible) or radiation (EB, gamma or beta).
- the present invention also relates to an impregnated wood element, wherein it is obtainable by impregnating a wood element with a composition in the form of a mixture or a mixture of the components of the composition in batch form, and thereafter curing the composition or the mixture. It has been explained above, that the mixture of the components of the composition in batch form as defined above is the equivalence of the composition in the form of a mixture as defined above.
- the present invention thus relates to an impregnated wood element, which is obtainable by impregnating a wood element with a composition in the form of a mixture comprising at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol selected from the group consisting of mercaptopropionate esters, mercaptoacetate esters and mixtures thereof, and component b) comprises at least one mono and/or multifunctional ene chosen from the group consisting of norbornene, vinyl ether, propenyl, alkene, vinyl ester, N-vinyl amides, allyl ethers, allyltriazine, allylisocyanurate, acrylate, unsaturated esters, N-substituted meleimide, acrylonitrile, methacrylate, styrene, conjugated dienes and mixtures thereof, the molar ratio between the thiol groups and the ene groups is 1:0.1 to 1:1
- the composition for the impregnation method may have all properties disclosed above.
- the impregnated wood element may be a compressed wood element.
- the impregnated wood element achieves excellent properties when impregnated with the composition or the mixture according to the present invention.
- Several tests have been executed by the independent technological institute SWEREA IVF of Gothenburg. Hardness tests were preformed on several hard species. The results are shown in Example 8.
- the test shows that ordinary hard wood achieves significantly increased mechanical properties with respect to hardness that increases up to 600%, and bending strength that increases up to 70%.
- the hardness for alder increased from 2.1 Brinell to 15-2 Brinell and for birch the hardness increased from 2.6 Brinell to 14.9 Brinell.
- the bending strength for birch increased from 115 MPa to 160 MPa and for alder the bending strength increased from 90 MPa to 121 MPa.
- the compressed (according to the Calignum patent EP 0729401 B1) impregnated wood samples achieves up 300% increase in hardness and up to 150% increase in bending strengths.
- the hardness for compressed beech increased from 7.2 Brinell to 11.7 Brinell and for compressed birch increased from 4.5 Brinell to 11.9 Brinell.
- the bending strength for compressed birch increased from 141 MPa to 239 MPa and for compressed beech increased from 175 MPa to 202 MPa.
- All wood elements impregnated according to this patent can be processed (sanding, flattening, sawing etc) similar to extra hard natural wood. This means that the wood elements can be processed in any wood tool or machinery. However, as the impregnated wood now is very hard, the tools need to be sharpened/maintained accordingly.
- the impregnated wood will also have increased dimension stability and water resistance.
- the impregnated wood element may comprise from about 1 to about 80% by weight of the composition or the mixture calculated on the total weight of the impregnated wood element. This is a wide interval for the amount of composition that may be taken up of the wood. A low amount may be useful for only giving an already hard and mechanically good wood element a nice colour, an improved protection for water, while the wood may already have a quite good resistance to water. Further, a very porous wood type may take up about 80% by weight of the composition. This might be necessary for getting the desired properties of such a wood element. If the wood element is porous, it needs to be strengthened by the composition. It also may need an increased water resistance in this extent obtainable by the high amount of composition. The amount of the composition or the mixture which is taken up by the wood element depends on the selected wood and the composition. Further, it is regulated by the method, which is described below.
- the method of impregnating a wood element may also comprise a step of subjecting the wood element for some kind of compression.
- the compression may be performed before or after the impregnation step.
- the wood element can be subjected to compression in any direction of the wood element.
- the wood element can be selected from the group consisting of soft wood and hard wood. Both kinds of wood will work. Examples of soft wood are pine and spruce. Hard wood may be birch, alder, aspen, beech or oak.
- the wood element are ideal for most indoor wood products like flooring, stairs and furniture that utilize a hard, beautiful surface with a high degree of resistance to wear and tear. Generally all indoor wood constructions will benefit from the increased mechanical properties like bending strength. The increased water resistance combined with the increased strength makes it a good material for out door use, such as wood for building constructions, outdoor furniture etc.
- the present invention also relates to a method of impregnating wood, wherein the wood is impregnated with a composition in the form of a mixture according to the present invention or a mixture of the components of the composition in batch form (multi-component form) according to the present invention.
- the present invention then may relate to a method of impregnating a wood element, wherein the wood element is impregnated with a composition in the form of a mixture comprising at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol selected from the group consisting of mercaptopropionate esters, mercaptoacetate esters and mixtures thereof, and component b) comprises at least one mono and/or multifunctional ene chosen from the group consisting of norbornene, vinyl ether, propenyl, alkene, vinyl ester, N-vinyl amides, allyl ethers, allyltriazine, allylisocyanurate, acrylate, unsaturated esters, N-substituted meleimide, acrylonitrile, methacrylate, styrene, conjugated dienes and mixtures thereof, the molar ratio between the thiol groups and the ene groups is 1:0.1
- the present invention may relate to a method of impregnating a wood element, wherein the wood element is impregnated with a mixture of a composition in batch form comprising at least two components a) and b), wherein component a) comprises at least one mono and/or multifunctional thiol selected from the group consisting of mercaptopropionate esters, mercaptoacetate esters and mixtures thereof, and component b) comprises at least one mono and/or multifunctional ene chosen from the group consisting of norbornene, vinyl ether, propenyl, alkene, vinyl ester, N-vinyl amides, allyl ethers, allyltriazine, allylisocyanurate, acrylate, unsaturated esters, N-substituted meleimide, acrylonitrile, methacrylate, styrene, conjugated dienes and mixtures thereof, the molar ratio between the thiol groups and the ene groups is 1:0.1
- the components a) and b) may be mixed just before the impregnation.
- composition in the start of the latter method is in a batch composition, wherein the two components a) and b) are separate from each other.
- the two components a) and b) are mixed with each other to a mixture.
- the composition of the two components is a mixture already at the beginning of the method.
- the components usually react faster with each other and have a shorter pot life.
- Impregnation of wood is easily understood by a person well known in the art. Impregnation generally involves the steps of applying vacuum and pressure in an autoclave to achieve penetration of the impregnation liquid into the wood product. The impregnated wood is then typically cured through the use of heat to accomplish polymerization of the impregnation fluid (within the wood cell structures). Even though the method is commonly known, some examples of how to achieve the impregnation is described below.
- the wood element may be impregnated using the steps i, ii, iii, vii, viii and optionally one or more of the steps iv, v and vi in an arbitrary order.
- composition or the mixture can also be fed, under vacuum, into the chamber as an alternative process step.
- the wood element is than charged alone into the chamber before vacuum is applied.
- the other process steps are the same and can be applied in arbitrary order.
- the steps may be done in any suitable order. Thus, they are not necessary performed in the order disclosed above. Further, some of the steps may be performed twice or more. These methods are commonly used methods in impregnating wood elements.
- the step viii) which is the curing or heating step, is starting the curing of the composition.
- the curing can be performed at a temperature from room temperature up to about 180° C. However, even higher temperatures can be used and this is dependent on the wood substrate and thiolene composition.
- the heating and curing time depend on which components a) and b) that are used and on the temperature. Curing at room temperature makes it necessary to use a longer time for the curing.
- the amount of composition which can be taken up by the wood element can be adjusted by the different steps in the method.
- a lower vacuum may prepare the wood for an easy take up of composition and a high over pressure may force the composition into the wood element.
- the duration of different steps may also influence the amount of composition which is taken up by the wood element.
- the present invention relates to the use of a composition in the form of a mixture according to the present invention as disclosed above or a mixture of the components of the composition in batch form according to the present invention as disclosed above for impregnating a wood element.
- the invention especially relates to the use of a composition in the form of a mixture comprising at least two components a) and b); or a mixture of at least two components a) and b) of a composition in batch form, wherein the components a) and b) are separated from each other before use; wherein component a) comprises at least one mono and/or multifunctional thiol selected from the group consisting of mercaptopropionate esters, mercaptoacetate esters and mixtures thereof, and component b) comprises at least one mono and/or multifunctional ene chosen from the group consisting of norbornene, vinyl ether, propenyl, alkene, vinyl ester, N-vinyl amides, allyl ethers, allyltriazine, allylisocyanurate, acrylate, unsaturated esters, N-substituted meleimide, acrylonitrile, methacrylate, styrene, conjugated dienes and mixtures thereof, the
- compositions of the thiol TMPMP and different enes in molar ratio 1:1 between the thiol groups and the ene groups where tested and different speeds of the reaction were noted.
- the compositions were placed in vessels. The temperature was first at RT (room temperature, 20° C.) up to 20 minutes, thereafter at 78° C. up to 25 minutes and finally at 100° C. until the reaction was completed (curing). Sometimes it was not necessary to heat to the higher temperatures, since the composition was already cured (FTIR, conversion of double bonds>90%.
- FTIR measures the conversion of double bonds in %. Hardness is measured by pressure of a pen towards the surface and bending the specimen.
- compositions of different thiols and the ene TMPTA in molar ratio 1:1 between the thiol groups and the ene groups where tested and different speeds of the reaction were noted.
- the compositions were placed in vessels. The temperature was at 80° C. until the reaction was completed (curing means>90% conversion of double bonds measured by FTIR).
- TMPMP Trimethylolpropane Tri-3-mercaptopropionate
- TMPTA Trimethylolpropane Triacrylate
- the effect of different curing temperatures was investigated with a composition of the thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the ene TMPTA (Trimethylolpropane Triacrylate).
- the molar ratio was 1:1 between the thiol and ene groups.
- Wooden pieces of compressed alder (50 ⁇ 150 ⁇ 4 mm) were impregnated with the composition above.
- the impregnation process parameters were the following:
- Vacuum pressure 0.2 bar during 4 minutes
- Curing was performed in a convection oven at different temperatures and times. See table 3a and 3b.
- Table 3c is an additional example shown.
- the composition in the investigation was thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the ene TMPTMA (Trimethylolpropane Trimethacrylate).
- the molar ratio was 1:5.6 between the thiol and ene groups.
- Wooden pieces of compressed alder (50 ⁇ 150 ⁇ 4 mm) were impregnated with the composition above.
- the impregnation process parameters were the following:
- Vacuum pressure 0.1 bar during 6 minutes
- composition in the investigation was thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the ene TMPTA (Trimethylolpropane Triacrylate).
- the molar ratio was 1:1.3 between the thiol and ene groups.
- Wooden pieces of compressed alder (50 ⁇ 150 ⁇ 4 mm) were impregnated with the composition above.
- the impregnation process parameters were the following:
- Vacuum pressure 0.1 bar during 10 minutes
- Table 6 shows results from examples of impregnation of different types of wood which are both natural and compressed.
- composition in the investigation was thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the enes TMPTMA (Trimethylolpropane Trimethacrylate) and HDDA (Hexanedioldiacrylate), the molar ratio between the enes are 8:2. The molar ratio was 1:2 between the thiol and ene groups.
- Wooden pieces (2000 ⁇ 200 ⁇ 4 mm) were impregnated with the composition above.
- the impregnation process parameters were the following:
- the thiolene impregnation process is according to the examples above and the tests show that it can be used for all type of woods.
- the wood can be both natural and compressed.
- a coloured composition is obtained by using dyes, micronized pigments and/or pigments. Examples are shown below for natural or compressed wood impregnated with coloured compositions having properties that are equal or better than wood from rain forest.
- the composition in the investigation was thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the enes TMPTMA (Trimethylolpropane Trimethacrylate) and TEGDA (Triethyleneglycoldiacrylate), the molar ratio between the enes are 9:1. The molar ratio was 1:2 between the thiol and ene groups. To the composition was added an orange dye and a black dye.
- the ordinary hard wood achieves significantly increased mechanical properties with respect to hardness that has an extra-high increase (up to 600%) and bending strength that has a high increase (up to 70%).
- the compressed (according to the Calignum patent EP 0729401B1) impregnated wood samples achieves medium-high increase in hardness (up to 300%) and a high to extra-high increase in bending strength (up to 150%).
- the table 9 below show different amount of thiolene composition in wood elements ranging from 0 to 80% by weight.
- the composition in the investigation was thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the enes TMPTMA (Trimethylolpropane Trimethacrylate) and HDDA (Hexandioldiacrylate), the molar ratio between the enes are 9:1.
- the molar ratio was 1:2 between the thiol and ene groups.
- Wooden pieces (2000 ⁇ 200 ⁇ 4 mm) were impregnated with the composition above.
- the impregnation process parameters were the following:
- the table 10 below show different molar ratios between thiol and ene in wood elements ranging from 1:0.1 to 1:100.
- the composition in the investigation was thiol TMPMP (Trimethylol-propane Tri-3-mercaptopropionate) and the ene TMPTMA (Trimethylolpropane Trimethacrylate.
- Wooden pieces (2000 ⁇ 200 ⁇ 4 mm) were impregnated with the composition above.
- the impregnation process parameters were the following:
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US9062210B2 (en) | 2011-07-20 | 2015-06-23 | Empire Technology Development Llc | Compositions and methods for making glass fortified wood |
EP2623281A1 (fr) * | 2012-01-31 | 2013-08-07 | Titan Wood Limited | Bois acétylé |
WO2013159096A1 (fr) * | 2012-04-20 | 2013-10-24 | Clarkson University | Procédés de polymérisation aqueuse de thiol-ène |
CN103625147B (zh) * | 2013-10-29 | 2016-05-04 | 安徽唯宝印刷科技有限公司 | 一种印刷用橡皮布还原剂 |
WO2017116820A1 (fr) | 2015-12-31 | 2017-07-06 | 3M Innovative Properties Company | Articles et compositions durcissables de points quantiques |
US11015114B2 (en) | 2015-12-31 | 2021-05-25 | 3M Innovative Properties Company | Article comprising particles with quantum dots |
CN107081836A (zh) * | 2017-05-06 | 2017-08-22 | 阜南县腾祥工艺品有限公司 | 一种木碗加工制作的方法 |
CN107009468A (zh) * | 2017-05-12 | 2017-08-04 | 阜南县腾祥工艺品有限公司 | 一种木制垫子制作的方法 |
CN107009471A (zh) * | 2017-05-12 | 2017-08-04 | 阜南县腾祥工艺品有限公司 | 一种木制的铲子的制作方法 |
CN108582349A (zh) * | 2018-04-19 | 2018-09-28 | 苏州凌科特新材料有限公司 | 一种耐热木质复合材料的制备方法 |
CN110698672A (zh) * | 2019-10-30 | 2020-01-17 | 贵州民族大学 | 一种通过可见光引发硫醇-烯点击反应制备的多重响应性树枝化聚硫醚聚合物及其方法 |
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RU2009117164A (ru) | 2010-11-10 |
RU2535949C2 (ru) | 2014-12-20 |
US20090280344A1 (en) | 2009-11-12 |
PL2128199T3 (pl) | 2012-11-30 |
WO2009136824A1 (fr) | 2009-11-12 |
EP2128199B1 (fr) | 2012-06-13 |
JP5616031B2 (ja) | 2014-10-29 |
EP2128199A2 (fr) | 2009-12-02 |
CA2665285C (fr) | 2016-08-16 |
CA2665285A1 (fr) | 2009-11-06 |
EP2128199A3 (fr) | 2010-10-20 |
ES2391746T3 (es) | 2012-11-29 |
JP2009269403A (ja) | 2009-11-19 |
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